Canonical Allele Identifier: CA386926703
Community Standard Title: NM_181486.4(TBX5):c.756-2A>G
Gene: TBX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114366393T>C , CM000674.2:g.114366393T>C GRCh38
NC_000012.11:g.114804198T>C , CM000674.1:g.114804198T>C GRCh37
NC_000012.10:g.113288581T>C NCBI36
NG_007373.1:g.47050A>G , LRG_670:g.47050A>G

Transcript Alleles

HGVS Amino-acid Change
NM_181486.4:c.756-2A>G MANE Select NP_852259.1:n.756-2A>G
ENST00000405440.7:c.756-2A>G MANE Select ENSP00000384152.3:n.756-2A>G
NM_000192.3:c.756-2A>G , LRG_670t1:c.756-2A>G NP_000183.2:n.756-2A>G
NM_080717.2:c.606-2A>G NP_542448.1:n.606-2A>G
NM_080717.3:c.606-2A>G NP_542448.1:n.606-2A>G
NM_080717.4:c.606-2A>G NP_542448.1:n.606-2A>G
NM_181486.2:c.756-2A>G NP_852259.1:n.756-2A>G
ENST00000310346.8:c.756-2A>G ENSP00000309913.4:n.756-2A>G
ENST00000349716.9:c.606-2A>G ENSP00000337723.5:n.606-2A>G
ENST00000405440.6:c.756-2A>G ENSP00000384152.2:n.756-2A>G
ENST00000526441.1:c.756-2A>G ENSP00000433292.1:n.756-2A>G
XM_017019912.1:c.804-2A>G XP_016875401.1:n.804-2A>G